Transcriptome analyses of taste organoids reveal multiple pathways involved in taste cell generation

Sci Rep. 2017 Jun 21;7(1):4004. doi: 10.1038/s41598-017-04099-5.

Abstract

Taste cells undergo constant turnover throughout life; however, the molecular mechanisms governing taste cell generation are not well understood. Using RNA-Seq, we systematically surveyed the transcriptome landscape of taste organoids at different stages of growth. Our data show the staged expression of a variety of genes and identify multiple signaling pathways underlying taste cell differentiation and taste stem/progenitor cell proliferation. For example, transcripts of taste receptors appear only or predominantly in late-stage organoids. Prior to that, transcription factors and other signaling elements are upregulated. RNA-Seq identified a number of well-characterized signaling pathways in taste organoid cultures, such as those involving Wnt, bone morphogenetic proteins (BMPs), Notch, and Hedgehog (Hh). By pharmacological manipulation, we demonstrate that Wnt, BMPs, Notch, and Hh signaling pathways are necessary for taste cell proliferation, differentiation and cell fate determination. The temporal expression profiles displayed by taste organoids may also lead to the identification of currently unknown transducer elements underlying sour, salt, and other taste qualities, given the staged expression of taste receptor genes and taste transduction elements in cultured organoids.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Morphogenetic Proteins / genetics
  • Cell Differentiation / genetics
  • Cell Lineage / genetics
  • Cell Proliferation / genetics*
  • Gene Expression Regulation / genetics
  • Hedgehog Proteins / genetics
  • Male
  • Mice
  • Organoids / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, Notch / genetics
  • Signal Transduction / genetics
  • Stem Cells / metabolism
  • Taste / genetics*
  • Taste Perception / genetics*
  • Transcriptome / genetics*
  • Wnt Proteins / genetics

Substances

  • Bone Morphogenetic Proteins
  • Hedgehog Proteins
  • Receptors, G-Protein-Coupled
  • Receptors, Notch
  • Wnt Proteins